FDA Medical Device Recalls (openFDA)
Craftmatic Industries, Inc.: Legacy Base for Dual Bed Configurations
- Recall number
- Z-1500-2022
- Recalling firm
- Craftmatic Industries, Inc.
- Product
- Legacy Base for Dual Bed Configurations
- Status
- Open, Classified
- Initiated
- 2017-03-24
- Posted
- not on file
- Terminated
- not on file
- Reason
- A potential for dual-configured beds to separate or slip away from one another.
- Root cause
- Component design/selection
- Action
- The firm initiated the recall by email on 03/24/2017. The notice explained the issues and provided the following actions: "1. If your bed or beds is/are on a smooth surface or on carpeting that does not secure the position of the bed(s), we require that rubber castor cups be laced under the legs of the bed. 2. If you purchased a dual system (two beds side by side with two individual mattresses) and your beds are not connected so as to prevent separation, we will assist you in connecting them with our recommended strapping. Craftmatic will make appropriate arrangements to ensure that your dual system beds are properly connected or secured without cost to you. 3. If you no longer are in possession of the bed(s) you received form Craftmatic it is IMPORTANT that you provide Craftmatic with the contact information for the current user of the bed or beds. Likewise, if the bed has been discarded and is not available for use by anyone it is IMPORTANT that you inform Craftmatic. 4. It is IMPORTANT that Craftmatic receive confirmation that you have received this notification. To assist us in this regard please check or select one of the web links provided below. Selection the first option will automatically notify us that you have received ad read this notification. Selecting the second option will take you to a different webpage where you will be asked to answer a series of questions. That webpage will provide instruction for providing the required information. Proceed by selecting the Web Link Option 1 or 2 as applicable: 1. ___I received this notice and the information above does not apply. 2. ___I received this notice and will call in reference to the information above. Please Note: If your beds are installed with both rubberized castor cups and dual beds have been secured you must still notify us that you have received this notice and understand what is requested of you. RESOLUTION: Issue 1. If you require to be supplied with rubberized castor cups or need as
- Quantity
- not on file
- Distribution
- US Nationwide distribution - product was not distributed outside of the United States
- Lot, serial or model codes
- 4AT056, 4AT061, 4AT063
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- LLI
- Firm FEI
- 3008872045
- Firm city
- Pompano Beach
- Firm state
- FL
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28